{{Rsnum
|rsid=17172185
|Chromosome=7
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HECW1
|position=43247240
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HECW1,LOC102724911
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 1.8 | 8.8 | 89.4
| HCB | 5.1 | 34.3 | 60.6
| JPT | 5.3 | 51.3 | 43.4
| YRI | 0.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 5.1 | 34.3 | 60.6
| CHD | 2.8 | 46.8 | 50.5
| GIH | 0.0 | 4.0 | 96.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 3.5 | 7.0 | 89.5
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 25.5 | 74.5
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=24121790
  |Trait=Esophageal adenocarcinoma
  |Title=A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus.
  |RiskAllele=T
  |Pval=5E-6
  |OR=1.47
  |ORtxt=[1.25-1.75]
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}